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Treatment of Ventilator-associated Pneumonia with High-dose Colistin Under Continuous Veno-venous Hemofiltration

Tijdschriftbijdrage - Tijdschriftartikel

Background and Objectives: High-dose colistin (COL) ensures adequate treatment of pneumonia caused by multidrug resistant gram-negative bacteria (MDR-GNB) but must be weighed against a higher risk of nephrotoxicity. Continuous veno-venous hemofiltration (CVVH) clears COL by filtering and membrane adsorption that permits to avoid dose accumulation and excessively high peak concentrations. We evaluated clinical/microbiological efficacy of the high-dose COL treatment under CVVH in patients with newly diagnosed MDR-GNB ventilator-associated pneumonia (VAP).

Methods: Observational cohort study in critically ill adult patients with MDR-GNB VAP. Colistimethate sodium (CMS) was administered as a 9 million international units (MIU) of loading dose followed by 3 × 4.5 MIU daily. CVVH was performed over a highly adsorptive membrane. Clinical and microbiological efficacies were assessed at the end of therapy. In survivors, serum creatinine level was evaluated before and at the end of therapy.

Results: Fourteen patients (8 male patients, aged 57 ± 14 years) were consecutively included. Isolated pathogens were Pseudomonas aeruginosa in 7, Klebsiella pneumoniae in 5, and other Enterobacteriaceae in 2 patients. A favorable clinical response was observed in 9 patients (64%). Full and presumed microbiological eradication was observed in 12 patients (86%). Two patients were diagnosed with Stage 1 acute kidney injury.

Conclusions: In patients with MDR-GNB VAP, CVVH may represent an interesting option to enable effective high-dose COL treatment.

Tijdschrift: Journal of Translational Internal Medicine
ISSN: 2224-4018
Issue: 3
Volume: 7
Pagina's: 100-105
Jaar van publicatie:2019
Trefwoorden:acute kidney injury, colistin, continuous veno-venous hemofiltration, nephrotoxicity, ventilator-associated pneumonia
  • PubMed Central Id: PMC6795054
  • Scopus Id: 85086475829
  • DOI: https://doi.org/10.2478/jtim-2019-0022
  • ORCID: /0000-0002-2490-216X/work/63636080
  • ORCID: /0000-0002-7724-886X/work/63636947
  • WoS Id: 000491466600004
Toegankelijkheid:Open